Literature DB >> 6090971

Motor evoked potentials from transcranial stimulation of the motor cortex in cats.

W J Levy, M McCaffrey, D H York, F Tanzer.   

Abstract

Electrical testing of central nervous system pathways is assuming increasing importance in clinical medicine. However, there is no direct monitor of the motor system. We previously reported using a motor evoked potential created by direct excitation of the spinal cord, placing a stimulating electrode over the corticospinal tract area. To produce a less invasive test, we now use direct transcranial stimulation of the motor cortex through the scalp or direct stimulation of the motor cortex itself during operation. A descending signal can be recorded over the spinal cord and in the peripheral nerves where no retrograde sensory signals should be able to descend. This motor cortex stimulation produces contralateral limb movements and selective activation of the peripheral nerves of a limb. The characteristics of this signal are similar to those described in the neurophysiological literature for a descending motor signal. With a depth electrode, it was found that the signal was strongest in the spinal cord near the corticospinal tracts and in the anterior horn cell area. A set of lesioning studies showed that most of the signal travels in the area of the corticospinal tract, with some traveling in the ventral portion of the spinal cord, perhaps in the anterior corticospinal tract. Section of the pyramid essentially abolishes the signal, but lesioning of the red nucleus does not. This test offers an electrical assessment of the motor system that can be useful in experimental work on spinal cord and brain function. It has potential clinical applicability in humans.

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Year:  1984        PMID: 6090971     DOI: 10.1227/00006123-198408000-00011

Source DB:  PubMed          Journal:  Neurosurgery        ISSN: 0148-396X            Impact factor:   4.654


  13 in total

1.  Spinal cord ischemia and motor evoked potentials.

Authors:  D J Doyle
Journal:  J Clin Monit       Date:  1990-10

2.  Motor evoked potential monitoring during neurosurgical operations on the spinal cord.

Authors:  J Zentner
Journal:  Neurosurg Rev       Date:  1991       Impact factor: 3.042

3.  Motor versus somatosensory evoked potential changes after acute experimental spinal cord injury in rats.

Authors:  M Zileli; J Schramm
Journal:  Acta Neurochir (Wien)       Date:  1991       Impact factor: 2.216

Review 4.  Muscle relaxant use during intraoperative neurophysiologic monitoring.

Authors:  Tod B Sloan
Journal:  J Clin Monit Comput       Date:  2012-09-27       Impact factor: 2.502

5.  The role of bradykinin in the etiology of vasogenic brain edema and perilesional brain dysfunction.

Authors:  I R Whittle; I R Piper; J D Miller
Journal:  Acta Neurochir (Wien)       Date:  1992       Impact factor: 2.216

6.  Vestibulospinal evoked potential versus motor evoked potential monitoring in experimental spinal cord injuries of cats.

Authors:  M Zileli; M Taniguchi; C Cedzich; J Schramm
Journal:  Acta Neurochir (Wien)       Date:  1989       Impact factor: 2.216

7.  The contribution of arachidonic acid to the aetiology and pathophysiology of focal brain oedema; studies using an infusion oedema model.

Authors:  I R Whittle; I R Piper; J D Miller
Journal:  Acta Neurochir (Wien)       Date:  1991       Impact factor: 2.216

8.  A method of monitoring function in corticospinal pathways during scoliosis surgery with a note on motor conduction velocities.

Authors:  S G Boyd; J C Rothwell; J M Cowan; P J Webb; T Morley; P Asselman; C D Marsden
Journal:  J Neurol Neurosurg Psychiatry       Date:  1986-03       Impact factor: 10.154

9.  Corticospinal direct response in humans: identification of the motor cortex during intracranial surgery under general anaesthesia.

Authors:  Y Katayama; T Tsubokawa; S Maejima; T Hirayama; T Yamamoto
Journal:  J Neurol Neurosurg Psychiatry       Date:  1988-01       Impact factor: 10.154

10.  Neuropathological and neurophysiological effects of interstitial white matter autologous and non-autologous protein containing solutions: further evidence for a glioma derived permeability factor.

Authors:  I R Whittle; J W Ironside; I R Piper; J D Miller
Journal:  Acta Neurochir (Wien)       Date:  1993       Impact factor: 2.216

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